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Zimmer Biomet, Inc. recalls Biomet Small Diameter Cement Plug Inserter-Sterile, single-use accessory instrumentation to be used during surgical proc
Recalled April 10, 2019 · FDA recall Z-1081-2019 · Zimmer Biomet
Hazard
Lack of an adequate sterilization validation · FDA Class II
Units
89 units
Sold at
Nationwide
Description
Lack of an adequate sterilization validation
Product
Biomet Small Diameter Cement Plug Inserter-Sterile, single-use accessory instrumentation to be used during surgical procedures utilizing the Small Diameter Cement Plug implant devices Item Number: 414989
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →